Synthesis Characterization and Evaluation of Novel Substituted Azole Derivatives
Benzimidazole is a very stable nucleus and the derivatives of 2-methyl benzimidazole may show different and better biological activity. Thepresence of the thiazolidinone ring in a benzimidazole derivative enhances its antimicrobial activity. 2-methyl benzimidazole derivative are
formed by the condensation of o-phenylenediamine with acetic acid. Combination of two or more active moieties into one is a common
procedure, can result in augmenting the activity and removes untoward side effects. Hence, the present work focuses on synthesis of potent
antimicrobial benzimidazole derivatives by the condensation of Schiff's bases of 2-methyl benzimidazole moiety with thiomalic acid affording the
thiazolidinone ring and to study their antimicrobial activity. In antibacterial activity (Staphylococcus aureus and Escherichia coli), it shows that
compound TE6
is the most active compound and in antifungal activity (Candida albicans), TE3 & TE4 are found to be most active.
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